Iron−Sulfur Cluster Biosynthesis. Characterization of Frataxin as an Iron Donor for Assembly of [2Fe-2S] Clusters in ISU-Type Proteins
- 26 April 2003
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 125 (20) , 6078-6084
- https://doi.org/10.1021/ja027967i
Abstract
ISU (eukaryotes) and IscU (prokaryotes) are a homologous family of proteins that appear to provide a platform for assembly of [2Fe-2S] centers prior to delivery to an apo target protein. The intermediate [2Fe-2S] ISU-bound cluster is formed by delivery of iron and sulfur to the apo ISU, with the latter delivered through an IscS-mediated reaction. The identity of the iron donor has thus far not been established. In this paper we demonstrate human frataxin to bind from six to seven iron ions. Iron binding to frataxin has been quantitated by iron-dependent fluorescence measurements [KD(Fe3+) ≈ 11.7 μM; (KD(Fe2+) ≈ 55.0 μM] and isothermal titration calorimetry (ITC) [KD(Fe3+) ≈ 10.2 μM]. Enthalpies and entropies for ferric ion binding were determined from calorimetric measurements. Both fluorescence (KD 0.45 μM) and ITC measurements (KD 0.15 μM) demonstrate holo frataxin to form a complex with ISU with sub-micromolar binding affinities. Significantly, apo frataxin does not bind to ISU, suggesting an important role for iron in cross-linking the two proteins and/or stabilizing the structure of frataxin that is recognized by ISU. Holo frataxin is also shown to mediate the transfer of iron from holo frataxin to nucleation sites for [2Fe-2S] cluster formation on ISU. We have demonstrated elsewhere [J. Am. Chem. Soc. 2002, 124, 8774−8775] that this iron-bound form of ISU is viable for assembly of holo ISU, either by subsequent addition of sulfide or by NifS-mediated sulfur delivery. Provision of holo frataxin and inorganic sulfide is sufficient for cluster assembly in up to 70% yield. With NifS as a sulfur donor, yields in excess of 70% of holo ISU were obtained. Both UV−vis and CD spectroscopic characteristics were found to be consistent with those of previously characterized ISU proteins. The time course for cluster assembly was monitored from the 456 nm absorbance of holo ISU formed during the [2Fe-2S] cluster assembly reaction. A kinetic rate constant kobs ≈ 0.075 min-1 was determined with 100 μM ISU, 2.4 mM Na2S, and 40 μM holo frataxin in 50 mM Tris-HCl (pH 7.5) with 4.3 mM DTT. Similar rates were obtained for NifS-mediated sulfur delivery, consistent with iron release from frataxin as a rate-limiting step in the cluster assembly reaction.Keywords
This publication has 17 references indexed in Scilit:
- Iron−Sulfur Cluster Biosynthesis: Characterization of Iron Nucleation Sites for Assembly of the [2Fe−2S]2+ Cluster Core in IscU ProteinsJournal of the American Chemical Society, 2002
- Iron-Sulfur Cluster BiosynthesisPublished by Elsevier ,2002
- Transfer of Sulfur from IscS to IscU during Fe/S Cluster AssemblyJournal of Biological Chemistry, 2001
- The mitochondrial proteins Ssq1 and Jac1 are required for the assembly of iron sulfur clusters in mitochondriaJournal of Molecular Biology, 2001
- Crystal Structure of Human FrataxinJournal of Biological Chemistry, 2000
- Iron-Dependent Self-Assembly of Recombinant Yeast Frataxin: Implications for Friedreich AtaxiaAmerican Journal of Human Genetics, 2000
- Maturation of cellular Fe–S proteins: an essential function of mitochondriaTrends in Biochemical Sciences, 2000
- Inactivation of the Friedreich ataxia mouse gene leads to early embryonic lethality without iron accumulationHuman Molecular Genetics, 2000
- Recent advances in the molecular pathogenesis of Friedreich ataxiaHuman Molecular Genetics, 2000
- Studies of human, mouse and yeast homologues indicate a mitochondrial function for frataxinNature Genetics, 1997